Pyridine, 2,6-bis[(phenylthio)methyl]- is an organic compound characterized by a pyridine ring substituted at the 2 and 6 positions with phenylthio methyl groups. This compound features a nitrogen atom within the six-membered aromatic ring, which contributes to its basicity and potential for forming coordination complexes. The presence of the phenylthio groups enhances its lipophilicity and may influence its reactivity and solubility in organic solvents. Pyridine derivatives are often utilized in various chemical applications, including as ligands in coordination chemistry, intermediates in organic synthesis, and in the development of pharmaceuticals. The specific arrangement of substituents in this compound can affect its electronic properties, making it of interest in materials science and medicinal chemistry. Safety data should be consulted for handling, as compounds with sulfur and nitrogen functionalities can exhibit toxicity or environmental hazards. Overall, the unique structure of 2,6-bis[(phenylthio)methyl]-pyridine contributes to its diverse potential applications in chemical research and industry.

Pyridine, 2,6-bis[(phenylthio)methyl]-

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Tyrosinase-IN-33 (compound 5), a pyridine-based compound, acts as an effective inhibitor of diphenolase activity in mushroom tyrosinase. It significantly reduces enzyme activity with an IC50 of 9.0 μM.

CAS 137058-21-0: Pyridine, 2,6-bis[(phenylthio)methyl]-

Tyrosinase-IN-33

Ref: TM-T200002